Cytoplast RTM Collagen Bovine Resorbable Membrane Size: 30x40mm

Description:

Cytoplast RTM Collagen Bovine Resorbable Membrane in the 30x40mm size is a bovine collagen-based resorbable barrier membrane designed for appropriate dental regenerative procedures. The membrane is intended to provide temporary barrier coverage during guided bone regeneration and guided tissue regeneration workflows where separation of the treatment area from surrounding tissues is required. Measuring 30x40mm, this configuration provides the largest of the three RTM Collagen sizes listed here and is intended for situations where broader membrane coverage is appropriate. The product is supplied as two membranes per box. Its resorbable collagen construction means that the membrane is designed to gradually break down following placement, avoiding the routine need for a separate surgical procedure to remove a non-resorbable barrier.

The larger membrane dimensions provide dental professionals with additional material for coverage of appropriately sized treatment areas. Clinicians should determine the required membrane size based on the characteristics and dimensions of the treatment site, the intended procedure, and the applicable clinical protocol. Proper handling, positioning, adaptation, and stabilization should be performed according to the manufacturer's instructions for use. The Cytoplast RTM Collagen family offers different membrane dimensions so that dental professionals can select a configuration appropriate for the planned procedure.

The 30x40mm option can be distinguished from the 15x20mm and 20x30mm configurations by its larger surface area and packaging specification. Understanding these differences is important for dental inventory management and surgical preparation. The membrane is intended for professional use and should be handled with appropriate sterile technique. Dental teams should verify the product size and packaging before a procedure to ensure that the selected membrane matches the treatment plan. As with other regenerative biomaterials, the membrane should be used only according to its approved labeling and manufacturer instructions. Clinicians should review indications, contraindications, warnings, precautions, handling instructions, and storage requirements before use. Patient-specific factors and professional clinical judgment should guide the selection and application of the product.